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(Senior) QA Expert Manufacturing Oversight(m/w/x)
Quality oversight for sterile medicine manufacturing at global pharma company. GMP and aseptic manufacturing experience required. Relocation assistance, agile career path.
Requirements
- Solid experience in GMP controlled environment
- Experience in Quality Assurance
- Experience in Aseptic manufacturing
- Sound experience in deviation handling
- Ideally certified for deviation handling
- Experience in QA manufacturing oversight preferred
- Willingness to work in shifts
- Willingness to be present in manufacturing area
- Full gowning necessary
- Preferably daily presence in cleanroom
Tasks
- Ensure sterile manufacturing runs safely and smoothly
- Collaborate with production teams to identify and address issues
- Work in a cleanroom environment daily
- Establish and maintain quality oversight for sterile manufacturing
- Advise on GMP and compliance topics
- Implement and own the GMP Quality System
- Review and approve quality protocols and reports
- Oversee GMP-compliant material and personnel flows
- Lead GMP compliance activities
- Support and lead quality-related projects
- Develop QA tools and processes
- Represent QA during inspections and audits
- Serve as primary QA contact for compliance issues
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
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- LonzaFull-timeOn-siteSeniorStein (AR)
- Lonza
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(Senior) QA Expert Manufacturing Oversight(m/w/x)
Quality oversight for sterile medicine manufacturing at global pharma company. GMP and aseptic manufacturing experience required. Relocation assistance, agile career path.
Requirements
- Solid experience in GMP controlled environment
- Experience in Quality Assurance
- Experience in Aseptic manufacturing
- Sound experience in deviation handling
- Ideally certified for deviation handling
- Experience in QA manufacturing oversight preferred
- Willingness to work in shifts
- Willingness to be present in manufacturing area
- Full gowning necessary
- Preferably daily presence in cleanroom
Tasks
- Ensure sterile manufacturing runs safely and smoothly
- Collaborate with production teams to identify and address issues
- Work in a cleanroom environment daily
- Establish and maintain quality oversight for sterile manufacturing
- Advise on GMP and compliance topics
- Implement and own the GMP Quality System
- Review and approve quality protocols and reports
- Oversee GMP-compliant material and personnel flows
- Lead GMP compliance activities
- Support and lead quality-related projects
- Develop QA tools and processes
- Represent QA during inspections and audits
- Serve as primary QA contact for compliance issues
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Not a perfect match?
- Lonza
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